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Accession: PRJNA291460 ID: 291460

Homo sapiens (human)

Exome Sequencing of Clear Cell Endometrial Tumors and Paired Non-tumor Samples

See Genome Information for Homo sapiens
The purpose of this study was to identify somatic (tumor-specific) mutations in clear cell endometrial tumor exomes. The dataset was generated at the NIH Intramural Sequencing Center (NISC) and NHGRI by next generation sequencing the exomes of 16 de-identified primary tumor DNAs and matched non-tumor DNAs.
AccessionPRJNA291460; dbGaP: phs000967
TypeUmbrella project (Subtype:Authorized Access)
OrganismHomo sapiens[Taxonomy ID: 9606]
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo; Homo sapiens
SubmissionRegistration date: 30-Jul-2015
NHGRI
RelevanceMedical
Project Data:
Resource NameNumber
of Links
Sequence data
SRA Experiments32
Other datasets
BioSample32
Genotype and Phenotype (dbGaP)1
SRA Data Details
ParameterValue
Data volume, Gbases183
Data volume, Mbytes89544
Homo sapiens encompasses the following sub-project:
Project TypeNumber of Projects
Phenotype or Genotype1
BioProject
accession
OrganismTitle
PRJNA291461Homo sapiensExome Sequencing of Clear Cell Endometrial Tumors and Paired Non-tumor Samples (NATIONAL INSTITUTES OF HEALTH)

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